Effects of Foam Roller Versus KT Tape on Delayed Onset Muscle Soreness

Sponsor
Riphah International University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT06076356
Collaborator
(none)
24
1
2
5.6
4.3

Study Details

Study Description

Brief Summary

Objective of this study is to compare the effects of foam roller with KT tape on DOMS. The university going students will be divided in two groups, with one group receiving Kinesio Tape as intervention and other Foam Rolling as intervention. Pain and range of motion will be assessed before and after the intervention and the effects of both interventions will be compared.

Condition or Disease Intervention/Treatment Phase
  • Other: Foam Rolling
  • Other: Kinesio Taping
N/A

Detailed Description

Delayed Onset Muscle Soreness (DOMS) is a common phenomenon experienced after unaccustomed or intense physical activity, characterized by muscle discomfort, pain, and reduced range of motion. Various interventions have been conducted to alleviate DOMS symptoms, including the use of foam rollers and Kinesiology Tape (KT tape).

This randomized controlled clinical trial aims to compare the effects of foam roller and KT tape interventions on reducing DOMS and improving muscle recovery. The participants would go for a single session of High Intensity Interval Training (HIIT) to induce DOMS. Group-A participants would receive KT taping afterwards, while Group-B participants would receive foam rolling as intervention. Their effect would be measured using Visual Analog Scale (VAS), Tenderness Grading Scale, Knee Range of Motion (ROM) and Vertical Jump Height. This study delves into the applications and potential benefits of KT tape and foam roller in managing DOMS, shedding light on their effectiveness and how they can contribute to enhancing post-exercise recuperation and overall well-being.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
24 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Concurrent Parallel Randomized Clinical TrialConcurrent Parallel Randomized Clinical Trial
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Effects of Foam Roller Versus KT Tape on Delayed Onset Muscle Soreness
Actual Study Start Date :
Aug 15, 2023
Anticipated Primary Completion Date :
Nov 30, 2023
Anticipated Study Completion Date :
Jan 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group A

Foam Rolling Group

Other: Foam Rolling
Foam Roller for 90 seconds over anterior (quadriceps) and posterior (hamstrings) aspect of thigh.

Active Comparator: Group B

Kinesio Taping Group

Other: Kinesio Taping
Kinesio taping over anterior (quadriceps) and posterior (hamstrings) aspect of thigh.

Outcome Measures

Primary Outcome Measures

  1. Pain (VAS Score) [Baseline, after 24 hours, after 48 hours, and after 72 hours]

    Pain will be measured using Visual Analog Scale (VAS) ranging from zero (0=no pain) to ten (10=worst pain).

  2. Tenderness [Baseline, after 24 hours, after 48 hours, and after 72 hours]

    Tenderness will be measured using Tenderness Grading Scale ranging from zero (0=no tenderness) to four (4=severe tenderness).

Secondary Outcome Measures

  1. Knee Range of Motion (Flexion) [Baseline, after 24 hours, after 48 hours, and after 72 hours]

    Range of motion will be measured using Universal Goniometer

  2. Vertical Jump Height [Baseline, after 24 hours, after 48 hours, and after 72 hours]

    Vertical Jump Height will be measured using Vertec.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 36 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Individuals with normal BMI (18.5 to 25 Kg/m2)
Exclusion Criteria:
  • Individuals with history of metabolic or musculoskeletal disease.

  • Individuals with any recent acute injury.

  • Athletes exercising regularly and regular gymnasium going individuals.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Riphah International University (RIU) Islamabad Islamabad Capital Territory Pakistan 44000

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Noman Sadiq, MS-SPT, Riphah International University, Islamabad.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT06076356
Other Study ID Numbers:
  • REC/01615 Maria Nawaz
First Posted:
Oct 10, 2023
Last Update Posted:
Oct 13, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Riphah International University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 13, 2023